A linux programmer's 5-year-old daughter is seriously ill and needs to donate money.

Today, I saw this news on the csdn homepage and felt that the real life is cruel. It is said that this is an engineer who has worked in the embedded field, especially the ARM/Linux field for many years. If nothing happened, he would be an ordinary programmer like us, but now even if he sold a house, it would be hard to help his daughter. Fate is impermanence! It is reported that xiaoyifan's treatment cost is as high as 30-50 US dollars, a US Charity Foundation is organizing donations, some domestic media are also calling for donations, hope that competent people can help them one, below are some of their situations. For details, please visit these two websites:

Http://www.help-yifan.org/

Www.yifanfund.com

 

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Without losing the freedom to breathe and walk, Pan Yifan, who is about to celebrate his 5th birthday, will be able to run and breathe freely in the sun like other children.

In her vague memories, her biggest wish was to get a pair of beautiful roller skates. One day she could put on it and dance freely. However, life left her more memories of countless needles and masks. Every night, her young hands closely protected the oxygen mask, fearing the loss of the only bond that kept her life.

From the second day of her arrival in the new world, she was immediately taken to the first aid ward for a thoracic punction, and her breathing went wrong. After 15 days of treatment, finally, I got home with my parents.

The second time she was admitted to the hospital was one year and two months old, she could not walk, or even crawl, because of interstitial pneumonia, due to suspicion of alveolar protein deposition, her lungs were flushed twice. 18 days later, the hospital gave up her treatment, except her parents.

When she took her home, her throat was completely hoarse, except to see her mouth crying, could not hear a little bit of sound. What's wrong with xiaoyifan? Her parents don't know. They can only sell the only house and do their best to help their children get healthy through multiple channels.

They configured her oxygen machine to give her enough oxygen to her exhausted lungs. The brave little Yifan finally survived the difficult days and slowly recovered to self-breathing, when she was three years old, she could move her stool.

If everything can continue, the flowers of life will bloom on schedule. However, the god of fate only gave her a year, and she could not learn to walk independently, her lungs are no longer able to provide enough oxygen to the body and are moving towards fibrosis. She needs to take an oxygen mask all day to help her breathe, and her walking efforts have to be terminated, any aerobic activity puts a lot of pressure on her lungs.

 

 

 

Since then, the distance between her departure from the oxygen generator is no more than the length of a three-meter hollow gas pipe. All her life comes from TV, and she likes to watch cartoons, smile and cry together with the role in the cartoon, And she gradually understands what is kind, what is beautiful, what is brave, when she saw on TV that many of the children in the Sichuan earthquake had lost their homes, she knew they needed more help. Now, she is proud to keep the thank-you letter from the Red Cross.

She had a dream that one day she could breathe and walk freely, put on beautiful roller skates, and dance freely. We sincerely invite you to join us to help Xiao Yifan. Saving one person means saving the world.